# PredniSONE

NDC: 68071-2509
Generic name: PredniSONE
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200323

FDA application: ANDA080352

## Active ingredients

- PREDNISONE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2509"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2509
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca3e5394-ed5b-45a3-e053-2995a90ac0f3